1462351-67-2

Basic information

• Product Name: (1S,2S,5R)-(+)-neomenthyl neryl selenide
• Synonyms: (1S,2S,5R)-(+)-neomenthyl neryl selenide
• CAS NO: 1462351-67-2
• Molecular Weight: 355.466
• Mol File: 1462351-67-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,2S,5R)-(+)-neomenthyl neryl selenide(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,5R)-(+)-neomenthyl neryl selenide(1462351-67-2)
• EPA Substance Registry System: (1S,2S,5R)-(+)-neomenthyl neryl selenide(1462351-67-2)

Safety Data

• Hazardous Substances Data: 1462351-67-2(Hazardous Substances Data)

Upstream product

• 910660-22-9 (+)-dineomenthyl diselenide 
• 2230-82-2 menthyl tosylate 
• 2216-51-5 (-)-menthol 
• 20536-36-1 neryl chloride 
• 1462351-55-8 (1S,2S,5R)-(+)-neomenthyl selenol 

Downstream Products

• 126-91-0 linalool 
• 126-90-9 (S)-(+)-linalool 

Relevant articles and documents

Synthesis and reactions of the optically active selenols derived from monoterpenes Dedicated to Professor Jacek Gawronski on the occasion of his 70th birthday

A convenient methodology for the synthesis of optically active selenols, derived from p-menthane, carane, and pinane, is described. The selenols were oxidized with air to give the optically active diselenides, and were also converted into the corresponding allylic selenides via reaction with Z- and E-cinnamyl, geranyl, and neryl chlorides. Oxidation of the allylic selenides with mCPBA gave the optically active alcohols via [2,3]-sigmatropic rearrangement of the in situ generated allylic selenoxides.